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Autism genes keep turning up chromatin
scientific article published on June 2013
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scholarly article
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Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
title
Autism genes keep turning up chromatin
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
main subject
autism
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author name string
Janine M Lasalle
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
publication date
1 June 2013
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stated in
Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
published in
OA autism
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Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
volume
1
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Europe PubMed Central
PMC publication ID
3882126
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20 August 2017
issue
2
1 reference
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Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
page(s)
14
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Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
cites work
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23 August 2017
Sex-biased gene expression in the developing brain: implications for autism spectrum disorders
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PubMed Central
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23 August 2017
Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits
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PubMed Central
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23 August 2017
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PubMed Central
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23 August 2017
The neuron-specific chromatin regulatory subunit BAF53b is necessary for synaptic plasticity and memory
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Emerging roles for chromatin as a signal integration and storage platform
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O-GlcNAc transferase (OGT) as a placental biomarker of maternal stress and reprogramming of CNS gene transcription in development
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Macro domains as metabolite sensors on chromatin.
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23 August 2017
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
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23 August 2017
Cytokine dysregulation in autism spectrum disorders (ASD): possible role of the environment
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Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulation
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23 August 2017
De Novo Gene Disruptions in Children on the Autistic Spectrum
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Patterns and rates of exonic de novo mutations in autism spectrum disorders
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23 August 2017
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
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23 August 2017
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
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23 August 2017
R-loop formation is a distinctive characteristic of unmethylated human CpG island promoters
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23 August 2017
Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation.
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23 August 2017
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Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-β-catenin signaling pathway
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23 August 2017
Epigenetic signatures of autism: trimethylated H3K4 landscapes in prefrontal neurons
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23 August 2017
Fragile x syndrome
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23 August 2017
Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci
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PubMed Central
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23 August 2017
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
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PubMed Central
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23 August 2017
Large-scale methylation domains mark a functional subset of neuronally expressed genes.
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PubMed Central
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Facioscapulohumeral muscular dystrophy: molecular pathological advances and future directions
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PubMed Central
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23 August 2017
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
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PubMed Central
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23 August 2017
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
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PubMed Central
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23 August 2017
A genome-wide scan for common alleles affecting risk for autism
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23 August 2017
Developmental regulation and individual differences of neuronal H3K4me3 epigenomes in the prefrontal cortex
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23 August 2017
ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain
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23 August 2017
Hypothesis: a unifying mechanism for nutrition and chemicals as lifelong modulators of DNA hypomethylation
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PubMed Central
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23 August 2017
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Human DNA methylomes at base resolution show widespread epigenomic differences
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PubMed Central
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23 August 2017
Epigenetics and environmental chemicals
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PubMed Central
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23 August 2017
Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
T cell receptor signaling controls Foxp3 expression via PI3K, Akt, and mTOR.
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23 August 2017
Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis
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PubMed Central
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23 August 2017
Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
A novel variant of the putative demethylase gene, s-JMJD1C, is a coactivator of the AR
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PubMed Central
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23 August 2017
The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Mutation analysis of methyl-CpG binding protein family genes in autistic patients
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
X-inactivation profile reveals extensive variability in X-linked gene expression in females
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Methyl-CpG binding protein MBD1 couples histone H3 methylation at lysine 9 by SETDB1 to DNA replication and chromatin assembly
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?
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PubMed Central
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23 August 2017
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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23 August 2017
Poly(ADP-ribose) polymerase 1 is inhibited by a histone H2A variant, MacroH2A, and contributes to silencing of the inactive X chromosome.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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14 September 2017
Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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2 September 2018
Plasticity of Foxp3(+) T cells reflects promiscuous Foxp3 expression in conventional T cells but not reprogramming of regulatory T cells.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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2 September 2018
Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882126
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2 September 2018
A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD)
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24404383
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.13172/2052-7810-1-2-610
1 reference
stated in
Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
PMC publication ID
3882126
1 reference
stated in
Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
PubMed publication ID
24404383
1 reference
stated in
Europe PubMed Central
PMC publication ID
3882126
retrieved
20 August 2017
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